| 8653602 | CV130177 | single nucleotide variant | NM_001033677.1(CABP1):c.1087+931C>T | Lung cancer [RCV000110664] | uncertain significance | 12 | 120662149 | 120662149 | Human | | name |
| 8653603 | CV130178 | single nucleotide variant | NM_001033677.1(CABP1):c.1088-2227C>T | Lung cancer [RCV000110665] | uncertain significance | 12 | 120664648 | 120664648 | Human | | name |
| 156180678 | CV2331473 | single nucleotide variant | NM_001033677.2(CABP1):c.127A>T (p.Thr43Ser) | not specified [RCV004184105] | uncertain significance | 12 | 120640812 | 120640812 | Human | | name |
| 156184359 | CV2349923 | single nucleotide variant | NM_001033677.2(CABP1):c.274C>T (p.Arg92Trp) | not specified [RCV004206336] | uncertain significance | 12 | 120640959 | 120640959 | Human | | name |
| 156252388 | CV2232398 | single nucleotide variant | NM_001033677.2(CABP1):c.536T>G (p.Leu179Arg) | not specified [RCV004099025] | uncertain significance | 12 | 120641221 | 120641221 | Human | | name |
| 156257105 | CV2369301 | single nucleotide variant | NM_001033677.2(CABP1):c.852T>A (p.Asp284Glu) | not specified [RCV004208213] | uncertain significance | 12 | 120660753 | 120660753 | Human | | name |
| 156108397 | CV2390234 | single nucleotide variant | NM_001033677.2(CABP1):c.991A>C (p.Met331Leu) | not specified [RCV004240612] | uncertain significance | 12 | 120661122 | 120661122 | Human | | name |
| 401773535 | CV2695276 | single nucleotide variant | NM_001033677.2(CABP1):c.935G>A (p.Arg312Gln) | not specified [RCV004303405] | uncertain significance | 12 | 120660836 | 120660836 | Human | | name |
| 401719948 | CV2705584 | single nucleotide variant | NM_001033677.2(CABP1):c.839A>G (p.His280Arg) | not specified [RCV004318448] | uncertain significance | 12 | 120660740 | 120660740 | Human | | name |
| 597750391 | CV3640755 | single nucleotide variant | NM_001033677.2(CABP1):c.892A>G (p.Thr298Ala) | not specified [RCV004892574] | uncertain significance | 12 | 120660793 | 120660793 | Human | | name |
| 597762615 | CV3640756 | single nucleotide variant | NM_001033677.2(CABP1):c.874C>A (p.Pro292Thr) | not specified [RCV004895187] | uncertain significance | 12 | 120660775 | 120660775 | Human | | name |